Nonuniform probability of glutamate release at a hippocampal synapse.

A change in the probability of neurotransmitter release (Pr) is an important mechanism underlying synaptic plasticity. Although Pr is often assumed to be the same for all terminals at a single synapse, this assumption is difficult to reconcile with the nonuniform size and structure of synaptic terminals in the central nervous system. Release probability was measured at excitatory synapses on cultured hippocampal neurons by analysis of the progressive block of N-methyl-D-aspartate receptor-mediated synaptic currents by the irreversible open channel blocker MK-801. Release probability was nonuniform (range of 0.09 to 0.54) for terminals arising from a single axon, the majority of which had a low Pr. However, terminals with high Pr are more likely to be affected by the activity-dependent modulation that occurs in long-term potentiation.

[1]  T. H. Brown,et al.  Evoked neurotransmitter release: statistical effects of nonuniformity and nonstationarity. , 1976, Proceedings of the National Academy of Sciences of the United States of America.

[2]  C. Cotman,et al.  Baclofen selectively inhibits excitatory synaptic transmission in the hippocampus , 1981, Brain Research.

[3]  H Korn,et al.  Transmission at a central inhibitory synapse. II. Quantal description of release, with a physical correlate for binomial n. , 1982, Journal of neurophysiology.

[4]  P G Nelson,et al.  Active and inactive central synapses in cell culture. , 1986, Journal of neurophysiology.

[5]  K. Harris,et al.  Membrane structure at synaptic junctions in area CA1 of the rat hippocampus , 1986, Neuroscience.

[6]  B. Bean,et al.  Block of N-methyl-D-aspartate-activated current by the anticonvulsant MK-801: selective binding to open channels. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[7]  B. Walmsley,et al.  Nonuniform release probabilities underlie quantal synaptic transmission at a mammalian excitatory central synapse. , 1988, Journal of neurophysiology.

[8]  C. Stevens,et al.  NMDA and non-NMDA receptors are co-localized at individual excitatory synapses in cultured rat hippocampus , 1989, Nature.

[9]  C. Stevens,et al.  Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[10]  C. Stevens,et al.  Presynaptic mechanism for long-term potentiation in the hippocampus , 1990, Nature.

[11]  R. Tsien,et al.  Presynaptic enhancement shown by whole-cell recordings of long-term potentiation in hippocampal slices , 1990, Nature.

[12]  S. Redman Quantal analysis of synaptic potentials in neurons of the central nervous system. , 1990, Physiological reviews.

[13]  R. Nicoll,et al.  Mechanisms generating the time course of dual component excitatory synaptic currents recorded in hippocampal slices , 1990, Neuron.

[14]  J. D. Clements,et al.  Activation kinetics reveal the number of glutamate and glycine binding sites on the N-methyl-d-aspartate receptor , 1991, Neuron.

[15]  D. Faber,et al.  Quantal analysis and synaptic efficacy in the CNS , 1991, Trends in Neurosciences.

[16]  C. Stevens,et al.  Excitatory and inhibitory autaptic currents in isolated hippocampal neurons maintained in cell culture. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[17]  M. Segal,et al.  Epileptiform activity in microcultures containing one excitatory hippocampal neuron. , 1991, Journal of neurophysiology.

[18]  G. Westbrook,et al.  The time course of glutamate in the synaptic cleft. , 1992, Science.

[19]  C. Jahr,et al.  High probability opening of NMDA receptor channels by L-glutamate. , 1992, Science.

[20]  K. Stratford,et al.  Presynaptic release probability influences the locus of long-term potentiation , 1992, Nature.

[21]  R. Nicoll,et al.  Postsynaptic contribution to long-term potentiation revealed by the analysis of miniature synaptic currents , 1992, Nature.

[22]  Kristen M. Harris,et al.  Quantal analysis and synaptic anatomy — integrating two views of hippocampal plasticity , 1993, Trends in Neurosciences.

[23]  P. Dutar,et al.  Presynaptic inhibitory effect of baclofen on hippocampal inhibitory synaptic transmission involves a pertussis toxin-sensitive G-protein. , 1993, European journal of pharmacology.

[24]  L. Trussell,et al.  Desensitization of AMPA receptors upon multiquantal neurotransmitter release , 1993, Neuron.